At a 50-year-old coal mine drainage barrens in central Pennsylvania, USA, we evaluated the biogeochemistry of acidic, Fe(III)oxy(hydr)oxide precipitates in reclaimed plots and compared them to untreated precipitates in control areas. Reclaimed plots supported successional vegetation that became established after a one-time compost and lime treatment in 2006, while control plots supported biological crusts. Precipitates were sampled from moist yet unsaturated surface layers in an area with lateral subsurface flow of mine drainage above a fragipan. Fe(II) concentrations were three- to five-fold higher in reclaimed than control precipitates. Organically bound Fe and amorphous iron oxides, as fractions of total Fe, were also higher in reclaimed than control precipitates. Estimates of Fe-reducing and Fe-oxidizing bacteria were four- to tenfold higher in root-adherent than both types of control precipitates. By scaling up measurements from experimental plots, total Fe losses during the 5-yr following reclamation were estimated at 45 t Fe ha−1 yr−1.

The current study aims to understand the speciation and fate of Cu complexes in hydrothermally altered sediments from the Central Indian Ocean Basin and assess the probable impacts of deep-sea mining on speciation of Cu complexes and assess the Cu flux from this sediment to the water column in this area. This study suggests that most of the Cu was strongly associated with different binding sites in Fe-oxide phases of the hydrothermally altered sediments with stabilities higher than that of Cu-EDTA complexes. The speciation of Cu indicates that hydrothermally influenced deep-sea sediments from Central Indian Ocean Basin may not significantly contribute to the global Cu flux. However, increasing lability of Cu-sediment complexes with increasing depth of sediment may increase bioavailability and Cu flux to the global ocean during deep-sea mining.

In this study, zinc oxide was immobilized on magnetite nanoparticles by chemical method and it was used as an adsorbent to remove reactive black 5 (RB5) dye from aqueous solution. The removal efficiency of RB5 was studied as the function of adsorbent dosage, pH, initial RB5 concentration, H₂O₂, and ionic strength (sodium carbonate, sodium bicarbonate, sodium sulfate, and sodium chloride). Removal efficiency of RB5 by ZnO–Fe₃O₄ was greater than that by ZnO and Fe₃O₄ in similar conditions. Maximum adsorption of ZnO–Fe₃O₄ was obtained at neutral pH, and adsorption capacity was estimated to be 22.1 mg/g. Adsorption kinetic study revealed that the pseudo-second-order model better described the removal rate than the pseudo-first-order model. Adsorption isotherm was analyzed by both Langmuir and Freundlich equations, and results showed that it was better described by the Langmuir equation. The removal efficiency of RB5 was increased with increasing initial H₂O₂ concentrations from 2 to 5 mM but was decreased above 5 mM. The adsorption capacities of RB5 was increased in the presence of NaCl but was greatly decreased in the presence of bicarbonate, carbonate, and sulfate ion. Adsorption activity of RB5 by ZnO–Fe₃O₄ composite was maintained even after five successive cycles, suggesting a promising adsorbent for wastewater-contaminated organic dyes.

Urban market gardening in Africa is suffering from increasing environmental contamination due to sources of contamination as varied as traffic, industry, and agriculture practices. A field study was therefore conducted to determine the global influence of the polluted environment (atmosphere, soil, and irrigation waters) on vegetable quality in a large urban-farming area. For leafy vegetables collected in 15 ha of squatted land belonging to the international airport of Cotonou, total concentrations of metal(loid)s measured in consumed parts of Lactuca sativa L. and Brassica oleracea were 52.6–78.9, 0.02–0.3, 0.08–0.22, 12.7–20.3, 1.8–7.9, and 44.1–107.8 mg kg⁻¹for Pb, Cd, As, Sb, Cu, and Zn, respectively. Human gastric bioaccessibility of the metal(loid)s was measured, and the obtained values varied according to the considered metal(loid) and the plant species. The results identified values that are commonly found in non-polluted soils and roots associated with contaminated edible parts, raising the possibility of atmospheric contamination. Such a hypothesis is in agreement with values of magnetic susceptibility, since iron oxides and probably their associated metal(loid)s do not translocate from the roots toward the upper parts of the plants. (Bioaccessible) estimated dose intake ((B)EDI) and total (bioaccessible) target hazard quotient (Σ(B)THQ) were calculated to assess the health risk of consuming vegetables from this area. Pb and Sb were the major risk contributors. Taking the bioaccessible fractions into account, ΣBTHQ values were lower than ΣTHQ but were all still >1 for both males and females, leading to the conclusion that consuming these vegetables from this area is not risk-free.

Redox conditions play an outstanding role in controlling the behaviour of trace elements in soil environments. They are not only sensitive to water saturation but also to soil temperature because many redox reactions are mediated by microorganisms. In this study, we investigated the influence of oxidising (oxygen predominant), weakly reducing (Mnᴵᴵᴵ,ᴵⱽreduction) and moderately reducing (Feᴵᴵᴵreduction) conditions at three temperature regimes (7, 15 and 25 °C) on the solubility of ten trace elements. Multimetal-contaminated topsoil (pH 5.8) from a floodplain in Germany was investigated with the following aqua regia-soluble concentrations: Zn 903, Cu 551, Cr 488, Pb 354, Ni 93.5, As 35.7, Co 22.4, Sb 20.5, Cd 8.3 and Mo 6.5 mg kg⁻¹. Soil suspensions were held at fixed redox potential in microcosm experiments, sampled at every third day and analysed for trace elements. Time to achieve weakly and particularly moderately reducing conditions was temperature dependent and increased in the order 25 °C < 15 °C < 7 °C. Under oxidising conditions, the solubility of the trace elements was low. Reductive dissolution of Mn oxides under weakly reducing conditions was accompanied by a release of Co and Mo. Reductive dissolution of Fe oxides (and of remaining Mn oxides) under moderately reducing conditions additionally led to a release of As, Cd, Cr, Ni and Pb, whereas Cu and Zn were hardly affected. Antimony revealed a different behaviour because, after a first increase, a continuous decrease in its concentration was observed soon after the onset of weakly reducing conditions. We conclude that soil temperature should be considered as a master variable, to distinguish between weakly and moderately reducing soil conditions, and that it is necessary to keep element-specific behaviour in mind when dealing with the effects of redox conditions in soils on trace element solubility.

A granular media synthesized using iron oxide nanoparticle-coated alumina (IONA) has been demonstrated as an effective solid catalyst in the heterogeneous catalytic ozonation of para-chlorobenzoic acid (pCBA). TEM analysis showed that iron oxide nanoparticles with an average size of 5–20 nm were well-coated onto an alumina surface. It was determined that the iron oxide nanoparticle coating increased the specific surface area by 54 times and the functional group density by 1.5 times. During catalytic ozonation at acidic pH levels, it was clearly observed that IONA increased the degradation of pCBA (98 %) through effective hydroxyl radical formation compared to bare alumina (9 %) under continuous ozonation processes. In comparing the Rcₜvalue, which represents the ratio of ozone exposure to hydroxyl radical exposure, the Rcₜof IONA was approximately four times higher than for bare alumina. In addition, IONA showed good stability for catalytic ozonation of pCBA in the reusability tests.

The use of magnetic micro- and nanoparticles for the removal of pollutants from wastewater is gaining increasing attention. Here, amine-functionalized magnetic microparticles (AFMMs) and carboxylic-functionalized magnetic microparticles (CFMMs) were synthesized by modifying the surface of Fe₃O₄with amino and carboxyl groups for fast and efficient removal of textile dyes from aqueous solution. The functionalized magnetic microparticles were characterized by TEM, SEM, FTIR, and VSM. The adsorption experiments were carried out by varying the regulating parameters like solution pH and adsorbent dosage and analyzed in terms of kinetic and isotherm models. It was demonstrated that simple electrostatic interactions between functionalized magnetic microparticles and adsorbates played a dominating role in the adsorption of textile dyes. The positively charged AFMMs adsorbed the negatively charged dyes vat blue (VB) and direct violet (DV) at pH 6 with the maximum removal percentages of 95.72 and 97.29 %, respectively. The maximum removal percentages of cationic dyes methylene blue (MB) and azure A chloride (AA) on the negatively charged CFMMs were 92.28 and 92.22 % at pH 11, respectively. Moreover, the adsorbed dyes could be desorbed completely from the surface of CFMMs at a lower pH, and AFMMs also allowed rapid removal of VB and DV in different water samples. All the results in the present work demonstrated that the functionalized magnetic microparticles as efficient, magnetically separable adsorbents are attractive for the removal of dye pollutants.

A new method for the degradation of bisphenol A (BPA) in aqueous solution was developed. The oxidative degradation characteristics of BPA in a heterogeneous Fenton reaction catalyzed by Fe₃O₄/graphite oxide (GO) were studied. Transmission electron microscopic images showed that the Fe₃O₄nanoparticles were evenly distributed and were ∼6 nm in diameter. Experimental results suggested that BPA conversion was affected by several factors, such as the loading amount of Fe₃O₄/GO, pH, and initial H₂O₂concentration. In the system with 1.0 g L⁻¹of Fe₃O₄/GO and 20 mmol L⁻¹of H₂O₂, almost 90 % of BPA (20 mg L⁻¹) was degraded within 6 h at pH 6.0. Based on the degradation products identified by GC–MS, the degradation pathways of BPA were proposed. In addition, the reused catalyst Fe₃O₄/GO still retained its catalytic activity after three cycles, indicating that Fe₃O₄/GO had good stability and reusability. These results demonstrated that the heterogeneous Fenton reaction catalyzed by Fe₃O₄/GO is a promising advanced oxidation technology for the treatment of wastewater containing BPA.

The zero-valent iron (ZVI) corrosion products and their functions were investigated in the combined ZVI and anaerobic sludge system. Results showed that ZVI corrosion occurred, and the reductive transformation and dechlorination of p-chloronitrobenzene (p-ClNB) by the anaerobic sludge were enhanced. In the combined systems with different types of ZVIs and mass ratios of anaerobic sludge to ZVI, a considerable amount of suspended iron compounds was produced and coated onto the microbial cells. However, the microbial cellular structure was damaged, and the p-ClNB reductive transformation was affected adversely after the long-term presence of nanoscale ZVI (NZVI) or reduced ZVI (RZVI) with a high concentration of 5 g L⁻¹. The oxidized products of FeOOH and Fe₃O₄were found on the surface of ZVI, which are speculated to act as electron mediators and consequently facilitate the utilization of electron donors by the anaerobic microbes.

The aim of our studies was to determine the efficiency of decomposition of non-ionic surfactant by the Fenton method in the presence of iron nanocompounds and to compare it with the classical Fenton method. The subject of studies was water solutions of non-ionic detergent Tergitol TMN-10 used in textile industry. Water solutions of the surfactant were subjected to treatment by the classical Fenton method and to treatment in the presence of iron nanocompounds. In the samples of liquid solutions containing the surfactant, chemical oxygen demand (COD) and total organic carbon (TOC) were determined. The Fenton process was optimized based on studies of the effect of compounds used in the treatment, doses of iron and nanoiron, hydrogen peroxide and pH of the solution on surfactant decomposition. Iron oxide nanopowder catalyzed the process of detergent decomposition, increasing its efficiency and the degree of mineralization. It was found that the efficiency of the surfactant decomposition in the process with the use of iron nanocompounds was by 10 to 30 % higher than that in the classical method. The amounts of formed deposits were also several times smaller.